Acupuncture/Moxibustion for Peripheral Neuropathy in HIV
National Center for Complementary and Integrative Health (NCCIH)
Information provided by (Responsible Party)
National Center for Complementary and Integrative Health (NCCIH)
First received: April 20, 2006
Last updated: September 16, 2009
Last Verified: September 2009
History of Changes
This is a sample-size-limited, randomized, blinded (subject and evaluator), sham acupuncture/placebo moxibustion (sham acu/placebo moxa) controlled clinical trial. The subjects in this study will be 50 men and women with HIV infection who have a diagnosis of distal symmetric peripheral neuropathy (DSP). Subjects will be randomized to one of two experimental intervention conditions:
- Condition 1: subjects receive acu/moxa treatment; and
- Condition 2 (Control Group): subjects receive sham acu/placebo moxa.
Procedure : Acupuncture/Moxibustion
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
|Official Title:||Acu/Moxa for Peripheral Neuropathy in Persons With HIV|
Further study details as provided by National Center for Complementary and Integrative Health (NCCIH):
Primary Outcome Measures
- Symptom diary
- Gracely Pain Scale
- Subjective Peripheral Neuropathy Scale
- Clinical Global Impression Scale
- Neurological Assessment Form
|Study Start Date:||November 2005|
|Study Completion Date:||January 2009|
|Primary Completion Date:||January 2009 (Final data collection date for primary outcome measure)|
Subjects in this early-phase clinical trial will be 50 men and women with HIV infection who have a diagnosis of Distal Symmetric Peripheral neuropathy (DSP). This study is a prospective, randomized, sham/placebo controlled, blinded (subject and evaluator), parallel groups clinical trial. Subjects will be randomized to one of two experimental intervention conditions:
- Condition 1: subjects receive Acu/Moxa Treatment; and
- Condition 2 (Control Group): subjects receive Sham acupuncture/Placebo moxibustion (Sham Acu/Placebo Moxa).
Subjects in Conditions 1 and 2 will attend 16 scheduled sessions over 15 weeks. All subjects will: be blinded/masked to treatment assignments, attend the same number of protocol sessions, be administered the same instruments, and submit their symptom diaries for data entry and analysis. After a screening/intake session, randomization and treatment sessions will follow. There will be six weeks of twice weekly treatment sessions, and three follow-up sessions at weeks 9, 11 and 15. All conditions will be identical in duration and be administered by licensed acupuncturists trained in Traditional Chinese Medicine. The aims of this study include:
- To establish the feasibility of the combined Acupuncture/Moxibustion treatment for 6 weeks of twice weekly sessions, in order to reduce the pain related to DSP among persons with HIV/AIDS, and to estimate the effect size of the Acu/Moxa treatment for a future clinical study. Inclusion of 2-, 4-, and 8-week no-treatment follow-up sessions will establish the maintainability of benefit.
- To determine the effect of combined Acupuncture/Moxibustion treatment for 6 weeks of twice weekly sessions on reducing symptoms of DSP (aching or burning pain, "pins and needles" sensation, and numbness) among persons with HIV/AIDS.
- To determine the effect of the combined Acupuncture/Moxibustion treatment for 6 weeks of twice weekly sessions on patient-perceived DSP symptom improvement and quality of life.
- To evaluate the logistics of a CAM clinical trial on persons with HIV/AIDS experiencing
|Ages Eligible for Study:||18 Years to 70 Years|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Men and women who are HIV positive or Centers for Disease Control (CDC)-defined AIDS diagnosed subjects who are 18 years of age or older, and have a history of distal symmetrical peripheral neuropathy of the lower extremities (legs and feet) for two months or greater.
- Patients experiencing moderate pain severity.
- Verification from primary provider of subject's: HIV status, diagnosis of DSP, and agreement that patient is clinically suitable for the study.
- Individuals able to successfully complete a mini-mental status exam.
- Individuals who understand and agree to complete daily symptom diaries for the duration of the study.
- Individuals taking antiretroviral combinations must have completed an initial 8 weeks of a stable regime (same drug[s], dose, and frequency) prior to entry into the study.
- Individuals taking chronic pain medications must be on a stable regime (same drug, dose, and frequency) for at least twenty-one (21) days prior to entry into the study.
- Individuals on all other medications which may have neuropathy listed as a side effect must be on a stable regime (same drug[s], dose, and frequency) for at least 21 days prior to entry in the study.
- Individuals with an acute medical condition, i.e. pneumocystis carinii pneumonia, tuberculosis, and/or other opportunistic infections or conditions that would require medical attention.
- Individuals with diagnosis of diabetes mellitus, B-12 deficiency
- Topically applied medications to the lower extremities.
- Individuals with alcohol and/or substance dependence.
- Individuals with bleeding tendency
- Currently receiving treatment with corticosteroids
- Use of isoniazid (INH), dapsone, or metronidazole within 8 weeks prior to enrollment.
- Severe heart disease, uncontrolled high blood pressure, lung disease, or renal failure.
- Pregnant women
- Individuals receiving acupuncture currently and less than 6 months prior to enrollment.
- Individuals with a history of receiving moxibustion.
- Individuals currently receiving other types of complementary therapies such as herbs, massage, reiki, etc.
- Individuals with plans for travel, lifestyle change, or other activity that would
Contacts and LocationsChoosing to participate in a study is an important personal decision.Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00317291
Locations Show More
|United States, New York|
|Columbia University School of Nursing, Acupuncture Laboratory|
|New York, New York, United States, 10032|
Sponsors and CollaboratorsNational Center for Complementary and Integrative Health (NCCIH)
|Principal Investigator:||Joyce K Anastasi, PhD, DrNP||Columbia University|
|Responsible Party:||National Center for Complementary and Integrative Health (NCCIH)|
|ClinicalTrials.gov Identifier:||NCT00317291 History of Changes|
|Other Study ID Numbers:||R21AT003092|
|Study First Received:||April 20, 2006|
|Last Updated:||September 16, 2009|
Keywords provided by National Center for Complementary and Integrative Health (NCCIH):Acupuncture
Additional relevant MeSH terms:
Peripheral Nervous System Diseases
ClinicalTrials.gov processed this data on October 16, 2017
This information is provided by ClinicalTrials.gov.